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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">glazmag</journal-id><journal-title-group><journal-title xml:lang="ru">The EYE ГЛАЗ</journal-title><trans-title-group xml:lang="en"><trans-title>The EYE GLAZ</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2222-4408</issn><issn pub-type="epub">2686-8083</issn><publisher><publisher-name>Академия медицинской оптики и оптометрии</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.33791/2222-4408-2025-3-217-221</article-id><article-id custom-type="elpub" pub-id-type="custom">glazmag-701</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group></article-categories><title-group><article-title>Краевая дегенерация роговицы Терриена. Клинический случай</article-title><trans-title-group xml:lang="en"><trans-title>Terrien’s marginal degeneration. A clinical case report</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2071-9322</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гаврилова</surname><given-names>Т. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Gavrilova</surname><given-names>T. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гаврилова Татьяна Валерьевна, доктор медицинских наук, профессор, член-корреспондент РАН, заведующая кафедрой офтальмологии</p><p>614000, г. Пермь, ул. Пушкина, д. 85</p></bio><bio xml:lang="en"><p>Tatyana V. Gavrilova, Dr. Sci. (Med.), Professor, Cor­res­ponding Member of the Russian Academy of Sciences, Head of the Department of Ophthalmology</p><p>85 Pushkina Str., Perm, 614000</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0008-9702-2842</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Соловьева</surname><given-names>Л. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Solovyeva</surname><given-names>L. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Соловьева Лариса Игоревна, кандидат медицинских наук, доцент кафедры офтальмологии</p><p>614000, г. Пермь, ул. Пушкина, д. 85</p></bio><bio xml:lang="en"><p>Larisa I. Solovyeva, Cand. Sci. (Med.), Associate Professor, Depar­tment of Ophthalmology</p><p>85 Pushkina Str., Perm, 614000</p></bio><email xlink:type="simple">Larisasolovyeva@rambler.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Романова</surname><given-names>М. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Romanova</surname><given-names>M. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Романова Марина Евгеньевна, ординатор кафедры офтальмологии</p><p>614000, г. Пермь, ул. Пушкина, д. 85</p></bio><bio xml:lang="en"><p>Marina E. Romanova, Resident, Department of Oph­thalmology</p><p>85 Pushkina Str., Perm, 614000</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Пермский государственный медицинский университет имени академика Е.А. Вагнера</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Academician Ye.A. Vagner Perm State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>28</day><month>09</month><year>2025</year></pub-date><volume>27</volume><issue>3</issue><fpage>217</fpage><lpage>221</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Академия медицинской оптики и оптометрии, 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Академия медицинской оптики и оптометрии</copyright-holder><copyright-holder xml:lang="en">Академия медицинской оптики и оптометрии</copyright-holder><license xlink:href="https://www.theeyeglaz.com/jour/about/submissions#copyrightNotice" xlink:type="simple"><license-p>https://www.theeyeglaz.com/jour/about/submissions#copyrightNotice</license-p></license></permissions><self-uri xlink:href="https://www.theeyeglaz.com/jour/article/view/701">https://www.theeyeglaz.com/jour/article/view/701</self-uri><abstract><p>Актуальность. Краевая дегенерация роговицы Терриена – редкое заболевание. Важна правильная диагностика, что может вызывать затруднения у врача, т. к. каждый случай практически уникален. Цель: представить вниманию клинический случай краевой дегенерации роговицы Терриена. Описание случая. Пациент Д., 49 лет, обратился к врачу-офтальмологу Пермской краевой клинической больницы в августе 2023 г. с жалобами на наличие новообразований на обоих глазах. При биомикроскопии выявлено значительное истончение периферических нижних отделов роговицы обоих глаз с рубцеванием и прорастанием сосудов конъюнктивы с формированием ложного птеригиума. По данным авторефрактометрии выявлен обратный астигматизм обоих глаз. На оптической когерентной томографии (ОКТ) переднего отдела обоих глаз видна полость, стенки которой образованы истонченной роговицей, частью радужки. По данным ультразвуковой биометрии обоих глаз радужка подтянута к роговице с формированием иридо-корнеальных синехий в углу передней камеры с обеих сторон. На основании анамнеза заболевания, стандартного офтальмологического обследования, результатов ОКТ переднего отдела обоих глаз поставлен диагноз: краевая дегенерация роговицы Терриена, осложненная стафиломой. Заключение. Представленный клинический случай краевой дегенерации Терриена у мужчины 49 лет демонстрирует важность постановки правильного диагноза. Анамнез заболевания, клиническая картина укладываются в имеющиеся не­многочисленные описания данной патологии, дополнительные методы обследования – ОКТ и ультразвуковая биометрия повышают точность диагностики. Такие пациенты нуждаются в постоянном наблюдении.</p></abstract><trans-abstract xml:lang="en"><p>Background. Terrien’s marginal degeneration (TMD) is a rare corneal disorder. Accurate diagnosis is essential but often challenging due to its highly variable clinical presentation. Purpose: to present a clinical case of Terrien’s marginal degeneration. Case description. A 49-year-old male presented to the ophthalmology department at Perm Regional Clinical Hospital in August 2023 with complaints of growths on both eyes. Slit-lamp biomicroscopy revealed marked thinning of the inferior peripheral cornea in both eyes, accompanied by stromal scarring and conjunctival vascular ingrowth, forming a pseudopterygium. Autorefractometry showed against-the-rule astigmatism in both eyes. Anterior segment OCT of both eyes revealed a cavitary structure bounded by thinned corneal stroma and adjacent iris tissue. displaced anteriorly toward the cornea with the formation of iridocorneal synechiae in the anterior chamber angle bilaterally. Ultrasound biomicroscopy confirmed these findings. Based on the clinical history, comprehensive ophthalmologic examination, and anterior segment OCT data, a diagnosis of Terrien’s marginal degeneration complicated by corneal staphyloma was established. Conclusion. This clinical case of Terrien’s marginal degeneration in a 49-year-old male underscores the importance of accurate diagnosis. The disease course and clinical features are consistent with the limited published descriptions of this condition. Ancillary imaging techniques, including anterior segment OCT and ultrasound biomicroscopy, enhance diagnostic accuracy in atypical presentations. Patients with TMD require long-term ophthalmic follow-up.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>краевая дегенерация Терриена</kwd><kwd>краевой кератит</kwd><kwd>истончение роговицы</kwd><kwd>псевдоптеригиум</kwd><kwd>васкуляризация роговицы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Terrien’s marginal degeneration</kwd><kwd>marginal keratitis</kwd><kwd>corneal thinning</kwd><kwd>pseudopterygium</kwd><kwd>corneal neovascularization</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Frank. Dissertation, Marburg, 1896. (Quoted by Rupprecht, K, M. F. A. 1907. V. XLV. P. 34).</mixed-citation><mixed-citation xml:lang="en">Frank. Dissertation, Marburg, 1896. (Quoted by Rupprecht, K, M. F. A. 1907. V. XLV. P. 34).</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Gifford SR, Sanford R. 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